Antazoline Hydrochloride structure
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Common Name | Antazoline Hydrochloride | ||
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CAS Number | 2508-72-7 | Molecular Weight | 301.814 | |
Density | N/A | Boiling Point | 475.5ºC at 760 mmHg | |
Molecular Formula | C17H20ClN3 | Melting Point | 238 °C | |
MSDS | Chinese USA | Flash Point | 241.4ºC | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of Antazoline HydrochlorideAntazoline hydrochloride is a 1st generation antihistamine with also anticholinergic properties used to relieve nasal congestion and in eye drops. |
Name | N-benzyl-N-(4,5-dihydro-1H-imidazol-2-ylmethyl)aniline,hydrochloride |
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Synonym | More Synonyms |
Description | Antazoline hydrochloride is a 1st generation antihistamine with also anticholinergic properties used to relieve nasal congestion and in eye drops. |
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Related Catalog |
Boiling Point | 475.5ºC at 760 mmHg |
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Melting Point | 238 °C |
Molecular Formula | C17H20ClN3 |
Molecular Weight | 301.814 |
Flash Point | 241.4ºC |
Exact Mass | 301.134583 |
PSA | 27.63000 |
LogP | 3.26130 |
Vapour Pressure | 3.31E-09mmHg at 25°C |
Storage condition | Store at RT |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H312-H315-H319-H332-H335 |
Precautionary Statements | P261-P280-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi:Irritant; |
Risk Phrases | R20/21/22;R36/37/38 |
Safety Phrases | S26-S36 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | NJ2150000 |
HS Code | 2933290090 |
Precursor 0 | |
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DownStream 2 | |
HS Code | 2933290090 |
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Summary | 2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Method development for impurity profiling in SFC: The selection of a dissimilar set of stationary phases.
J. Pharm. Biomed. Anal. 111 , 333-43, (2015) Supercritical fluid chromatography (SFC) is drawing considerable interest as separation technique in the pharmaceutical industry. The technique is already well established in chiral separations both a... |
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Antinociceptive, anti-inflammatory and smooth muscle relaxant activities of the pyrrolo[3,4-d]pyridazinone derivatives: Possible mechanisms of action.
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Treatment of allergic conjunctivitis: results of a 1-month, single-masked randomized study.
Eur. J. Ophthalmol. 20(5) , 811-8, (2010) To compare the effects of topical antiallergic eyedrops in relieving the signs and symptoms of patients with allergic conjunctival pathology.In this multicenter, single-masked, randomized study, 240 p... |
Antazoline Hydrochloride |
hydrochloride salt of antazoline |
Antazoline HCl |
UNII-FP8Q8F72JH |
Fenazolina |
Antistine hydrochloride |
Histazine |
2-(N-Benzylanilinomethyl)-2-imidazoline Hydrochloride |
N-Benzyl-N-(4,5-dihydro-1H-imidazol-2-ylmethyl)aniline hydrochloride (1:1) |
Antazolinium chloratum |
N-benzyl-N-(4,5-dihydro-1H-imidazol-2-ylmethyl)-aniline,hydrochloride |
MFCD00058145 |
1H-Imidazole-2-methanamine, 4,5-dihydro-N-phenyl-N-(phenylmethyl)-, hydrochloride (1:1) |
EINECS 219-719-8 |
Phenazoline hydrochloride |
N-Benzyl-N-(4,5-dihydro-1H-imidazol-2-ylmethyl)-anilin,Hydrochlorid |
Antazoline (hydrochloride) |